Trials / Recruiting
RecruitingNCT06680934
CABP2 Patient Registry and Natural History Study
Patient Registry for Individuals With CABP2-Associated Hearing Loss
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 100 (estimated)
- Sponsor
- University Medical Center Goettingen · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
This registry is designed to collect comprehensive information about the molecular genetic diagnoses and clinical information of individuals with CABP2-associated hearing impairment to support a natural history study.
Detailed description
A patient registry, in both German and English languages, has been established for patients with hereditary hearing impairment due to variants in CABP2. The study is conducted in accordance with the current version of the Declaration of Helsinki. The study protocol and database structure have been approved by the Ethics Committee of the University Medical Center Goettingen.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Molecular genetic testing and audiometry | Genetic testing and audiometry are the interventions of interest |
Timeline
- Start date
- 2024-08-16
- Primary completion
- 2049-08-16
- Completion
- 2049-08-16
- First posted
- 2024-11-08
- Last updated
- 2026-01-27
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT06680934. Inclusion in this directory is not an endorsement.